Raina R, Schläppi M, Fedoroff N
Biology Department and Biotechnology Institute, Pennsylvania State University 16802, USA.
Novartis Found Symp. 1998;214:133-40; discussion 140-3, 163-7. doi: 10.1002/9780470515501.ch8.
Transcription and transposition of the maize Suppressor-mutator (Spm) transposon are epigenetically controlled. Methylation of specific element sequences prevents transcription and transposition in a heritable manner. Reactivation and demethylation occur in the presence of an active element, implying the existence of an element-encoded epigenetic activator. The methylation target sequences are the 0.2 kb promoter and an 0.35 kb GC-rich downstream sequence. Two Spm-encoded proteins, TnpA and TnpD, participate in transposition. In addition, TnpA has positive and negative regulatory activities. TnpA represses and activates the unmethylated and methylated Spm promoters, respectively, and it participates in the transient and heritable demethylation of the promoter and GC-rich region. There is evidence that TnpA-mediated repressor and epigenetic activator functions occur by different molecular mechanisms.
玉米抑制子-突变体(Spm)转座子的转录和转座受表观遗传控制。特定元件序列的甲基化以可遗传的方式阻止转录和转座。在活性元件存在的情况下会发生重新激活和去甲基化,这意味着存在一种元件编码的表观遗传激活剂。甲基化靶序列是0.2 kb的启动子和一个0.35 kb富含GC的下游序列。两种由Spm编码的蛋白质TnpA和TnpD参与转座。此外,TnpA具有正负调控活性。TnpA分别抑制和激活未甲基化和甲基化的Spm启动子,并且它参与启动子和富含GC区域的瞬时和可遗传去甲基化。有证据表明,TnpA介导的阻遏物和表观遗传激活剂功能是通过不同的分子机制发生的。